首页> 外文会议>Physiology, Function, and Structure from Medical Images pt.1; Progress in Biomedical Optics and Imaging; vol.7,no.29 >3D in-vivo imaging of GFP-expressing T-cells in Mice with non-contact Fluorescence Molecular Tomography
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3D in-vivo imaging of GFP-expressing T-cells in Mice with non-contact Fluorescence Molecular Tomography

机译:非接触式荧光分子层析成像技术在小鼠中表达GFP的T细胞的3D体内成像

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Optical tomography has been proposed as a promising technique for probing deep in tissue with many medical applications. Recently, the adaptation of fluorescent probes by the radiologists, gave rise to a new imaging tool in the area of molecular imaging. Optical tomography can, provide three-dimensional images of fluorescent concentrations inside living systems of sizes in the order of many cm. Our optical tomographer was based on a technique which is called Fluorescence Molecular Tomography (FMT) and can quantify fluorescent signals in mice. The imaging procedure is performed in a non-contact geometry so that living subjects of arbitrary shapes can be imaged with no fibers attached to them. We have developed a way to reconstruct the 3D surface of the subject and we use theoretical models to account for the propagation of the emerging signal in the free space. The system consists of a rotating sample holder and a CCD camera in combination with a laser-scanning device. An Argon-ion laser is used as the source and different filters are used for the detection of various fluorophores or fluorescing proteins. So far, we have observed of the distribution of GFP expressing T-lymphocytes in-vivo for the study of the function of the immune system in a murine model. Then we investigated the performance of the FMT setup to quantify the different amounts of migrated cells in the different organs by comparing our results with the FACS measurements. Further experiments included the measurement of the variations of the T cell's concentration in-vivo, over time.
机译:已经提出光学断层摄影术作为在许多医学应用中探测组织深部的有前途的技术。近来,放射学家对荧光探针的适应使分子成像领域出现了一种新的成像工具。光学体层摄影术可以提供大小约为几厘米的生物系统内部荧光浓度的三维图像。我们的光学层析成像仪基于一种称为荧光分子层析成像(FMT)的技术,可以量化小鼠中的荧光信号。成像过程以非接触几何形状进行,因此可以在不附着任何纤维的情况下对任意形状的生物进行成像。我们已经开发出一种方法来重建对象的3D表面,并使用理论模型来说明新兴信号在自由空间中的传播。该系统由旋转样品架和CCD摄像头与激光扫描设备组成。氩离子激光器用作光源,不同的滤光片用于检测各种荧光团或荧光蛋白。到目前为止,我们已经观察到了表达GFP的T淋巴细胞在体内的分布,以研究鼠模型中免疫系统的功能。然后,我们通过将我们的结果与FACS测量结果进行比较,研究了FMT设置的性能,以量化不同器官中不同数量的迁移细胞。进一步的实验包括测量体内T细胞浓度随时间的变化。

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